Prospect Research Coordinator - Jacksonville, FL

The Clinical Research Coordinator engages with site operations and assists in the development of the Rovia network, including planning, coordinating, and executing clinical studies in accordance with the protocol, · contracted scope of work, ICH/GCP, · sponsor, · CRO, · Rovia SOP ...

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The entry-level Clinical Research Coordinator engages with site operations and assists in the development of the Rovia network, including planning, coordinating, and executing clinical studies in accordance with the protocol, · participates in study start up activities · supports ...

Coordinates clinical research including planning and execution of studies and assists in site operations. · ...

The Clinical Research Coordinator engages with site operations and assists in the development of the Rovia network. · Supports site selection visits. · Participates in study start up activities. · ...

Clinical Research Coordinator - Float will facilitate timely coordination of daily clinical trial activities across multiple research projects and ensure trial protocol compliance. · ...

We are actively hiring Clinical Research Coordinators at our Jacksonville location. · The Clinical Research Coordinator assists Investigators in executing clinical research trials. · ...

We are actively hiring Clinical Research Coordinators at our Jacksonville, FL location to assist Investigators in executing Phase I, II, III and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines while providing an impeccab ...

The entry-level Clinical Research Coordinator assists in the development of the Rovia network by planning, coordinating and executing clinical studies. Supports site selection visits and participates in study start up activities. · Supports the preparation and conducting of site ...

We are seeking a detail-oriented Clinical Research Coordinator to oversee and support all phases of clinical trials involving investigational drugs and medical devices. · Manage all aspects of study coordination including participant recruitment, informed consent, visit schedulin ...

Conduct quality assurance reviews of clinical research documentation and oversee the maintenance of electronic regulatory binders in Veeva eRegulatory. Ensure data integrity and standardization across protocols, coordinate with research finance, compliance, and departmental teams ...

The Clinical Research Coordinator III (CRC III) coordinates assigned research studies and educational programs funded by federal grants. Performs functions necessary for successful completion of protocols including enrollment and follow-up visits. · Reviews and follows research p ...

To work as an integral member of the Rovia/Investigator site staff, maintaining the day-to-day operations and assist in the development of the Rovia network. · This includes planning, coordinating, and executing clinical studies in accordance with the protocol, · contracted scope ...

As a Clinical Research Coordinator at Mayo Clinic, you will independently coordinate complex clinical research protocols with minimal direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. · ...

The entry-level Clinical Research Coordinator engages with site operations and assists in the development of the Rovia network, including planning, coordinating, and executing clinical studies in accordance with the protocol, · contracted scope of work ICH/GCP sponsor CRO Rovia S ...

The Clinical Research Coordinator III (CRC III) is responsible for coordinating assigned research studies and educational programs funded by federal grants in the Department of Emergency Medicine. · ...

Coordinates complex clinical research protocols with minimal direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. · ...

The Clinical Research Coordinator III will conduct quality assurance reviews of clinical research documentation, ensure data integrity and standardization across protocols, oversee the maintenance of electronic regulatory binders in Veeva eRegulatory, and support readiness for sp ...

The Clinical Research Coordinator III is responsible for the coordination of assigned research studies and educational programs. · Reviews and follows research protocols to screen and enroll patients into IRB approved studies. · Performs study follow-up visits including phlebotom ...

The entry-level Clinical Research Coordinator engages with site operations and assists in the development of the Rovia networkDuties/Responsibilities: · Supports the preparation and conducting of site selection visits. · Participates in study start up activities, · including Sour ...